KCNC1‐related disorders: new de novo variants expand the phenotypic spectrum

A recurrent de novo missense variant in KCNC1, encoding a voltage‐gated potassium channel expressed in inhibitory neurons, causes progressive myoclonus epilepsy and ataxia, and a nonsense variant is associated with intellectual disability. We identified three new de novo missense variants in KCNC1 i...

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Detalles Bibliográficos
Autores principales: Park, Joohyun, Koko, Mahmoud, Hedrich, Ulrike B. S., Hermann, Andreas, Cremer, Kirsten, Haberlandt, Edda, Grimmel, Mona, Alhaddad, Bader, Beck‐Woedl, Stefanie, Harrer, Merle, Karall, Daniela, Kingelhoefer, Lisa, Tzschach, Andreas, Matthies, Lars C., Strom, Tim M., Ringelstein, Erich Bernd, Sturm, Marc, Engels, Hartmut, Wolff, Markus, Lerche, Holger, Haack, Tobias B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649617/
https://www.ncbi.nlm.nih.gov/pubmed/31353862
http://dx.doi.org/10.1002/acn3.50799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649617/
https://www.ncbi.nlm.nih.gov/pubmed/31353862
http://dx.doi.org/10.1002/acn3.50799

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